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This study was designed to define changes in peripheral blood and milk cell subpopulations during chronic S. aureus infection.
It was concluded that total lying time, lying synchrony, milk cell count and locomotion score are potential indicators for the assessment of dairy cow welfare in different housing environments.
The supernant was decanted and RNA was extracted from the milk cell pellet by the Trizol method (Invitrogen, Carlsbad, CA) according to the manufacturer instructions.
To support these results, we checked SMAR1, total p53 and acetylated p53 in various breast carcinoma cell line MCF7, Hbl-100 and MDA-MB-231 derived from breast epithelial fibro-adenoma, breast epithelial milk cell and IDC G-III respectively.
However, some milk cell samples were more similar to milk fat samples than they were to other milk cell samples.
"Apoptosis" was similarly enriched among milk cell transcripts (Benjamini p = 0.0004), suggesting that the milk cell pellet contained some dying cells.
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No cytokine mRNA was found in milk cells from uninfected mammary glands.
Native milk samples were separated into fraction 1 (aqueous extract of milk fat), fraction 2 (cell and fat free milk whey) and fraction 3 (milk cells).
The aim of this investigation was to examine the profile of human milk cells and cytokines from asthmatic compared to non-asthmatic mothers.
uberis were induced both in infiltrating somatic milk cells and in mammary epithelial cells, demonstrating that the latter cell type plays a role in milk production as well as immune responsiveness.
Staining of milk cells is the average of 11 different samples.
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CEO of Professional Science Editing for Scientists @ prosciediting.com